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2 "Chang-Ho Jeon"
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Original Articles
Clinico-pathologic Parameters for Prediction of Microsatellite Instability in Colorectal Cancer
Sang-Bong Jung, Han-IL Lee, Hoon-Kyu Oh, Im-Hee Shin, Chang-Ho Jeon
Cancer Res Treat. 2012;44(3):179-186.   Published online September 30, 2012
DOI: https://doi.org/10.4143/crt.2012.44.3.179
AbstractAbstract PDFPubReaderePub
PURPOSE
Although the incidence of microsatellite instability (MSI) accounts for 10-15% of cases of colorectal cancer, its clinical application for all colorectal cancers has widened. We attempted to identify clinical and pathological parameters that may be helpful in selection of patients with MSI-high (MSI-H).
MATERIALS AND METHODS
A total of 120 resected colorectal cancers were enrolled retrospectively for this MSI study. Polymerase chain reaction (PCR) and denaturing high performance liquid chromatography and/or real time PCR methods with five markers and immunohistochemistry (IHC) for MLH1 and MSH2 were performed for analysis of cancer and blood specimens. Clinico-pathologic parameters, including IHC, were investigated in order to determine their usefulness as predictive factors of MSI.
RESULTS
Among 120 cases of colorectal cancer, MSI was observed in 15 cases (12.5%), including 11 cases of MSI-H and four cases of MSI-low. Patients with MSI were younger, less than 50 years old, had a family history of cancer, Rt. sided colon cancer and/or synchronous multiple colorectal cancer, mucinous histologic type, and serum carcinoembryonic antigen group in the normal range. Results of multivariate analysis showed Bethesda guidelines, Rt. sided and/or synchronous multiple colorectal cancer, and negative expression of IHC for MLH1, which was consistently associated with MSI-H. MSI-H colorectal tumors have met at least one of these three parameters and their sensitivity and specificity were 100% and 72.5%, respectively.
CONCLUSION
Bethesda guidelines, tumor location, and negative expression of MLH1 protein are important parameters for selection of patients with colorectal cancers for MSI testing. MSI testing is recommended for patients showing any of these three parameters.

Citations

Citations to this article as recorded by  
  • Predicting mechanism of immune response in microsatellite instability colorectal cancer
    Peng Sun, Yusong Luan, Xuhao Cai, Qi Liu, Peide Ren, Pengpan Xin, Yonggang Yu, Bolun Song, Yangyang Wang, Huijing Chang, Haoyue Ma, Yinggang Chen
    Heliyon.2024; 10(6): e28120.     CrossRef
  • Comparison of histopathologic and clinical characteristics of microsatellite instability in colorectal adenocarcinomas and its impact on survival
    Bilal Tunçtürk, Ulaş Alabalik, Ayşe Nur Keleş
    Biotechnology & Biotechnological Equipment.2024;[Epub]     CrossRef
  • Interventional gastroenterology in oncology
    Vaibhav Wadhwa, Nicole Patel, Dheera Grover, Faisal S. Ali, Nirav Thosani
    CA: A Cancer Journal for Clinicians.2023; 73(3): 286.     CrossRef
  • Molecular profiling of the colon cancer in South-Eastern Romania
    Razvan Catalin Popescu, Cristina Tocia, Costel Brînzan, Georgeta Camelia Cozaru, Mariana Deacu, Andrei Dumitru, Nicoleta Leopa, Anca Florentina Mitroi, Anca Nicolau, Eugen Dumitru
    Medicine.2021; 100(1): e24062.     CrossRef
  • Potential Mechanism of Immune Evasion Associated with the Master Regulator ASCL2 in Microsatellite Stability in Colorectal Cancer
    Qian Yang, Guowei Huang, Liyan Li, Enmin Li, Liyan Xu, Carlo Cavaliere
    Journal of Immunology Research.2021; 2021: 1.     CrossRef
  • Genetic and epigenetic analysis of the beta-2-microglobulin gene in microsatellite instable colorectal cancer
    Zuzana Snahnicanova, Ivana Kasubova, Michal Kalman, Marian Grendar, Peter Mikolajcik, Eva Gabonova, Ludovit Laca, Martin Caprnda, Luis Rodrigo, Rachele Ciccocioppo, Peter Kruzliak, Lukas Plank, Zora Lasabova
    Clinical and Experimental Medicine.2020; 20(1): 87.     CrossRef
  • Expression and significance of miR-654-5p and miR-376b-3p in patients with colon cancer
    Ping Li, Jia-Xun Cai, Fei Han, Jie Wang, Jia-Jie Zhou, Kai-Wen Shen, Liu-Hua Wang
    World Journal of Gastrointestinal Oncology.2020; 12(4): 492.     CrossRef
  • Concomitant occurrence of primary renal non-Hodgkin lymphoma and a colon cancer
    Ji Li, Yabin Zou, Bin Wang, Xiangwei Meng, Xun Sun
    Medicine.2019; 98(10): e14802.     CrossRef
  • Meta-analysis of the molecular associations of mucinous colorectal cancer
    I S Reynolds, S J Furney, E W Kay, D A McNamara, J H M Prehn, J P Burke
    British Journal of Surgery.2019; 106(6): 682.     CrossRef
  • Association between clinicopathological characteristics and RAS mutation in colorectal cancer
    Johan Rimbert, Gaëlle Tachon, Audelaure Junca, Claire Villalva, Lucie Karayan-Tapon, David Tougeron
    Modern Pathology.2018; 31(3): 517.     CrossRef
  • Deficient mismatch repair and RAS mutation in colorectal carcinoma patients: a retrospective study in Eastern China
    Xiangyan Zhang, Wenwen Ran, Jie Wu, Hong Li, Huamin Liu, Lili Wang, Yujing Xiao, Xiaonan Wang, Yujun Li, Xiaoming Xing
    PeerJ.2018; 6: e4341.     CrossRef
  • Comparison of the eighth version of the American Joint Committee on Cancer manual to the seventh version for colorectal cancer: A retrospective review of our data
    Guo-Jun Tong, Gui-Yang Zhang, Jian Liu, Zhao-Zheng Zheng, Yan Chen, Ping-Ping Niu, Xu-Ting Xu
    World Journal of Clinical Oncology.2018; 9(7): 148.     CrossRef
  • Analysis of factors influencing molecular testing at diagnostic of colorectal cancer
    Quentin Thiebault, Gautier Defossez, Lucie Karayan-Tapon, Pierre Ingrand, Christine Silvain, David Tougeron
    BMC Cancer.2017;[Epub]     CrossRef
  • Genetic heterogeneity in synchronous colorectal cancers impacts genotyping approaches and therapeutic strategies
    Moritz Jesinghaus, Nicole Pfarr, Matthias Kloor, Volker Endris, Luca Tavernar, Alexander Muckenhuber, Magnus von Knebel Doeberitz, Roland Penzel, Wilko Weichert, Albrecht Stenzinger
    Genes, Chromosomes and Cancer.2016; 55(3): 268.     CrossRef
  • The Immune Biology of Microsatellite-Unstable Cancer
    Matthias Kloor, Magnus von Knebel Doeberitz
    Trends in Cancer.2016; 2(3): 121.     CrossRef
  • Stromal expression of miR-21 in T3-4a colorectal cancer is an independent predictor of early tumor relapse
    Won Kyung Kang, Jin Kwon Lee, Seong Taek Oh, Sung Hak Lee, Chan Kwon Jung
    BMC Gastroenterology.2015;[Epub]     CrossRef
  • KRASandBRAFgene mutations and DNA mismatch repair status in Chinese colorectal carcinoma patients
    Ju-Xiang Ye
    World Journal of Gastroenterology.2015; 21(5): 1595.     CrossRef
  • Colorectal cancer
    Hermann Brenner, Matthias Kloor, Christian Peter Pox
    The Lancet.2014; 383(9927): 1490.     CrossRef
  • AJCC Cancer Staging Manual 7th Edition Criteria for Colon Cancer: Do the Complex Modifications Improve Prognostic Assessment?
    Danielle M. Hari, Anna M. Leung, Ji-Hey Lee, Myung-Shin Sim, Brooke Vuong, Connie G. Chiu, Anton J. Bilchik
    Journal of the American College of Surgeons.2013; 217(2): 181.     CrossRef
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Detection of Lung Cancer using MAGE A1-6 and SSX4 RT-PCR Expression Profiles in the Bronchial Wash Fluid
Kwan-Ho Lee, Kyung-Chul Shin, Chae-Hun Lee, Sang-Hoon Jheon, Chang-Ho Jeon
Cancer Res Treat. 2007;39(2):69-73.   Published online June 30, 2007
DOI: https://doi.org/10.4143/crt.2007.39.2.69
AbstractAbstract PDFPubReaderePub
Purpose

Bronchial wash fluid may be a useful for detecting lung cancer. To increase the detection rates, we performed molecular analysis with using MAGE A1-6 and SSX4 RT-PCR on bronchial wash fluid specimens.

Materials and Methods

We obtained 57 lung cancer tissue specimens by bronchoscopic biopsy and 131 bronchial washes from 96 patients with lung cancer and 35 patients with benign lung diseases. The MAGE A1-6 and SSX4 gene expressions were investigated in the cancer tissue specimens and bronchial wash fluids. We evaluated the positive detection rates of these methods according to the cytology results and the clinical findings.

Results

For the cancer tissue specimens and the bronchial wash fluid, the positive detection rate of MAGE or SSX4 was 91.2% and 75.0%, respectively. Combined MAGE and SSX4 PCR and cytology tests showed an 83.3% detection rate for the bronchial wash fluid. From bronchial washes of patients with benign lung diseases, the positive rates of using MAGE or SSX4 was 11.4%. In the bronchial wash fluid of lung cancer patients, 66.7% of the peripheral cancers were detected by MAGE or SSX4, while examination with cytology did not detect any peripheral lung cancer.

Conclusion

The application of both MAGE and SSX4 showed high sensitivity and specificity for the detection of lung cancer. Thus, MAGE and SSX4 RT-PCR may be effectively utilized as additional methods to improve detection of lung cancer with using bronchial wash fluids.

Citations

Citations to this article as recorded by  
  • Characterization of Melanoma-Associated Antigen-A Genes Family Differential Expression in Non-Small-Cell Lung Cancers
    Shirin Karimi, Foroozan Mohammadi, Mihan Porabdollah, Seyed Amir Mohajerani, Kian Khodadad, Seyed Alireza Nadji
    Clinical Lung Cancer.2012; 13(3): 214.     CrossRef
  • Expression of MAGE A 1-6 and SSX 1-9 Genes in the Sputum and Cancer Tissue of the Lung Cancer Patients
    Yeun Jae Lee, Jang Hoon Lee, Jung Cheul Lee, Kwan Ho Lee
    Tuberculosis and Respiratory Diseases.2011; 70(4): 315.     CrossRef
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  • 44 Download
  • 2 Crossref
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